Quick Facts at a Glance
- Recall Date
- December 31, 2025
- Hazard Level
- HIGH
- Brand
- Wizcure Pharmaa Private
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Wizcure Pharmaa Private
- Product type
- Diagnostic Strips
- Model numbers
- All lots
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 31, 2025
Reported by FDA DRUG
March 4, 2026
RecallRadar source check
March 11, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Wizcure Pharmaa Private Limited or your healthcare provider for guidance. Notification method: Letter
About This Product
Bio Glo Fluorescein Sodium Ophthalmic Strips are used for diagnostic purposes in eye examinations. Healthcare providers often utilize these strips to detect corneal abrasions and other eye conditions.
Why This Is Dangerous
The lack of assurance of sterility means that these strips may harbor harmful bacteria or other pathogens, potentially leading to serious infections if used in patients' eyes.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers using these strips risk potential infections, which can lead to serious health complications. The recall also creates inconvenience for those needing alternative diagnostic solutions.
Practical Guidance
How to identify if yours is affected
- Check the packaging for the product name: Bio Glo Fluorescein Sodium Ophthalmic Strips.
- Verify if the strips were purchased after January 1, 2025.
- Look for any lot numbers or expiration dates that may be listed on the box.
Where to find product info
The lot number and expiration date are typically located on the side or bottom of the packaging.
What timeline to expect
Expect refund processing to take approximately 4-6 weeks after returning the product.
If the manufacturer is unresponsive
- Document all communication attempts with the company.
- Contact your healthcare provider for additional support.
- Consider filing a complaint with the FDA if there is no response.
How to prevent similar issues
- Always check for sterility assurance when purchasing medical products.
- Look for FDA approval or clearance on products before use.
- Consult with healthcare providers for reputable brands and products.
Documentation advice
Keep copies of receipts, correspondence with the company, and any medical records related to product use.
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Product Details
The recall affects Bio Glo Fluorescein Sodium Ophthalmic Strips USP, with 300 diagnostic strips per box. The product was manufactured by Omni Lens Pvt Ltd in Ahmedabad, India, and distributed by HUB Pharmaceuticals, LLC. The products were distributed nationwide in the USA.
Key Facts
- Recall date: December 31, 2025
- Reported date: March 4, 2026
- Quantity recalled: 50,400 boxes
- Manufacturer: Omni Lens Pvt Ltd, India
- Distributed by: HUB Pharmaceuticals, LLC
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Safety Guide
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